TY  - JOUR
ID  - pittir20448
UR  - http://d-scholarship-dev.library.pitt.edu/20448/
IS  - 10
A1  - Wipf, P
A1  - Soth, MJ
Y1  - 2002/05/16/
N2  - Matrix presented The convergent synthesis of the fully functionalized C(1)-C(18) segment 24 of the furanocembranes lophotoxin and pukalide was accomplished in 11 steps and 10% overall yield. The key step was a stereoselective conversion of alkynoate 21 to trimethylsilyl 2-alkenylfuran 22.
JF  - Organic Letters
VL  - 4
SN  - 1523-7060
TI  - Synthesis of the C(1)-C(18) segment of lophotoxin and pukalide. Control of 2-alkenylfuran (E/Z)-configuration
SP  - 1787 
AV  - public
EP  -  1790
ER  -